Complement receptor 1 gene (CR1) intragenic duplication and risk of Alzheimer’s disease

Population genetics of immune-related multilocus copy number variation in Native Americans

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Late onset Alzheimer’s disease genetics implicates microglial pathways in disease risk

(2017) Anastasia G. Efthymiou et al.   Molecular Neurodegeneration

Complement in the pathogenesis of Alzheimer’s disease

(2017) B. Paul Morgan   Seminars in Immunopathology

High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment

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Genomic variants, genes, and pathways of Alzheimer's disease: An overview

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Microglial genes regulating neuroinflammation in the progression of Alzheimer's disease

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Analysis of the Putative Role of CR1 in Alzheimer’s Disease: Genetic Association, Expression and Function

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Alzheimer's disease is associated with low density of the long CR1 isoform

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The EMBL-EBI bioinformatics web and programmatic tools framework

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Complement and Its Receptors: New Insights into Human Disease

(2014) V. Michael Holers   Annual Review of Immunology

Technical considerations for genotyping multi-allelic copy number variation (CNV), in regions of segmental duplication

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Meta-analysis of the association between CR1 polymorphisms and risk of late-onset Alzheimer's disease

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Transcriptome and genome sequencing uncovers functional variation in humans

(2013) Tuuli Lappalainen et al.   NATURE

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

(2013) Jean-Charles Lambert et al.   NATURE GENETICS

Complement receptor 1 coding variant p.Ser1610Thr in Alzheimer's disease and related endophenotypes

(2013) Caroline Van Cauwenberghe et al.   NEUROBIOLOGY OF AGING

A coding variant in CR1 interacts with APOE-ɛ4 to influence cognitive decline

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Genetic association of CR1 with Alzheimer's disease: A tentative disease mechanism

(2012) Lili-Naz Hazrati et al.   NEUROBIOLOGY OF AGING

Complement receptor 1 (CR1) and Alzheimer's disease

(2011) Helen Crehan et al.   IMMUNOBIOLOGY

Alzheimer's disease

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Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sites

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Fast, scalable generation of high-quality protein multiple sequence alignments using Clustal Omega

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Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

(2011) Adam C Naj et al.   NATURE GENETICS

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

(2011) Paul Hollingworth et al.   NATURE GENETICS

Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals

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Origins and functional impact of copy number variation in the human genome

(2009) Donald F. Conrad et al.   NATURE

Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease

(2009) Jean-Charles Lambert et al.   NATURE GENETICS

A robust statistical method for case-control association testing with copy number variation

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